TY  - CHAP
M1  - Book, Section
TI  - Glutaric Acidemia Type II (GA-II)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  progressive  neurologic  disorder  caused  by  a  genetically  transmitted  inborn  error  of  metabolism  in  which  the  body  cannot  oxidize  fatty  acids.  Typical  clinical  features  include  respiratory  distress,  heart  failure,  hypoglycemia,  acidosis,  muscular  hypotonia,  characteristic  sweaty  odorous  feet,  and  death  often  in  the  neonatal  period.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164070959
ER  -